NDC 63629-7982-01 - Flecainide Acetate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
63629-7982
Requested NDC
63629-7982-01
Package NDCs from labels
63629-7982-4, 63629-7982-1, 63629-7982-2, 63629-7982-3, 63629-7982-01
Manufacturer
Bryant Ranch Prepack
Effective date
2024-04-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Flecainide Acetate - Bryant Ranch PrepackBryant Ranch Prepack2024-04-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63629-7982-1Flecainide Acetate30 in 1 BOTTLETABLET305
63629-7982-2Flecainide Acetate60 in 1 BOTTLETABLET605
63629-7982-3Flecainide Acetate90 in 1 BOTTLETABLET905
63629-7982-4Flecainide Acetate180 in 1 BOTTLETABLET1805

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63629-7982FLECAINIDE ACETATE TABLET [BRYANT RANCH PREPACK]5Current NDC, Legacy NDC, 4 package rows20240502_2013e6ef-9141-42c3-8ea8-285840ecdd15.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-7982-3EA - Each63629-7982ef261638-6ef9-443a-ac72-f190f02759a812025-08-11

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 3 · 41 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Flecainide AcetateFLECAINIDE ACETATE TABLETBryant Ranch Prepack5dc5b522-f16f-4b3b-b325-f4ace495f9662023-11-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 886662
unii: M8U465Q1WQ

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.